Copyright: ©Author(s) 2026.
World J Gastrointest Surg. Nov 27, 2026; 18(11): 125637
Published online Nov 27, 2026. doi: 10.4240/wjgs.125637
Published online Nov 27, 2026. doi: 10.4240/wjgs.125637
Table 1 Diagnostic performance, heterogeneity and risk of bias of emergency point-of-care ultrasound applications in the acute abdomen
| Ref. | Population/setting | Operator | Reference standard | Diagnostic threshold | Sensitivity (95%CI) | Specificity (95%CI) | LR+/LR- | Studies/patients | Heterogeneity (%) | Risk of bias/certainty | Interpretation and limitations |
| SBO: Study-level meta-analysis (Gottlieb et al[9], 2018) | ED and inpatient adults with suspected SBO | Mixed (EP and others) | CT, surgery, or final diagnosis | Dilated loop > | 92.4% (89.0%-94.7%) | 96.6% (88.4%-99.1%) | 27.5/0.08 | 11/1178 | NR in retrievable text | QUADAS-2 not reported in retrievable text; no GRADE | Strong rule-in; study-level pooling may overestimate sensitivity |
| SBO: IPD meta-analysis (Shokoohi et al[10], 2023) | Multicentre ED, adults | EP (attending and resident) | CT/surgery/final diagnosis | Dilated loop > | 83.0% (71.7%-90.4%) | 93.0% (55.3%-99.3%) | 11.9 (1.2-114.9)/0.2 | 5/433 | NR in retrievable text | IPD design reduces reporting bias; no GRADE | Most conservative estimate; specificity CI so wide the parameter is effectively unestimated |
| SBO: Meta-analysis with QUADAS-2 (Motavaselian et al[30], 2024) | ED adults with suspected SBO | Mixed | CT/surgery/final diagnosis | Dilated loop > | NR here (see source) | 0.80 (0.77-0.83) | N/A | 21/1977 | 62% sensitivity; 88% specificity (both P < 0.01) | QUADAS-2: High risk for patient selection and flow/timing in several studies; Egger P = 0.04 | Specificity 16 points below the two estimates above; publication bias detected |
| SBO: Bedside-threshold analysis (Shokoohi et al[11], 2024) | ED adults | EP | CT/surgery | Loop > 2.75 cm (AUC = 0.76, 0.71-0.81); ≤ 1.7 cm 100% sensitivity; > | N/A | Approximately 90.7% at > 4 cm | N/A | IPD secondary analysis | N/A | Unvalidated threshold-derivation study | Candidate threshold only; no measurement convention specified; age/sex shift optimum (2.95 cm at ≥ 65 years) |
| Acute cholecystitis: EP-POCUS meta-analysis (Wilson et al[32], 2024) | ED adults, suspected acute cholecystitis | EP | Final diagnosis | Stones + wall > 3 mm + Murphy sign + pericholecystic fluid | 70.9% (62.3%-78.2%) | 94.4% (88.2%-97.5%) | 12.7/0.31 | 10 included; estimates from 7/1772 | NR in retrievable text | Not reported in retrievable text | Rule-in test; negative scan does not exclude |
| Acute cholecystitis: All-operator meta-analysis (Huang et al[25], 2023) | Mixed settings, all specialties (EP subgroup) | All operators; EP subgroup | Final diagnosis/pathology | As above | 71% (69%-72%); EP 71% (67%-74%) | 85% (84%-86%); EP 92% (90%-93%) | N/A | 40/8652 | 89.7% (87%-92%) | QUADAS-2: > 25% of studies high risk (case-control design, non-consecutive enrolment) | Operator specialty changes specificity by 7 points |
| Acute cholecystitis: Prospective TG18-adjudicated cohort (Nipitkul et al[33], 2026) | ED adults, high disease prevalence | EP | TG18 | POCUS criteria vs TG18 (wall > 3 mm vs ≥ 4 mm scales) | 86.6% (83.4%-89.4%) | 17.1% (12.5-22.5) | NR/NPV 37.0% | 1/783 | N/A (primary study) | Prospective; single reference standard | Discordant with pooled specificity of 85%-94%; only gallstones were significantly associated with confirmed disease |
| Gastric: ED intubation cohort (Asokan et al[27], 2023) | ED adults undergoing urgent intubation | EP | Aspiration-relevant gastric content | Antral CSA ≥ 9.27 cm² | 100% | 87% | N/A | 1/100 | N/A | Single-centre | Risk stratification against a surrogate endpoint, not diagnosis |
| Gastric: Fasting IPD meta-analysis (Perlas et al[26], 2024) | Fasting adults (reference range) | Trained sonographers | Endoscopic/measured volume | 95th-percentile CSA 9.9 cm² (9.4-10.4); volume 2.3 mL/kg (2.3-2.4) | Grade 0/1 → 98% probability below threshold | N/A | N/A | 12/1203 | NR in retrievable text | Reference-range derivation | Thresholds do not generalise across position or population |
| Free fluid: Ectopic pregnancy (Moore et al[31], 2007) | ED women, suspected ectopic pregnancy | EP | Operative intervention | Any free fluid in Morison's pouch | N/A | N/A | LR+ 112 (15-831) | 1/242 | N/A | Single-centre; estimate rests on 10 fluid-positive patients | Decisive rule-in in a high-pretest obstetric population only |
| Free fluid: Prehospital FAST meta-analysis (Lin et al[19], 2024) | Prehospital trauma | Prehospital providers | CT/laparotomy | Any free fluid | 0.596 (0.345-0.822) | 0.970 (0.953-0.983) | N/A | 6/1356 | 94%a | GRADE: Sensitivity very low (inconsistency, imprecision, publication bias); specificity high | Trauma population, indirect evidence for non-traumatic disease; indicates the sensitivity ceiling |
| Free fluid: Cochrane review, blunt trauma (Stengel et al[18], 2018) | Blunt thoracoabdominal trauma, adults and children | Mixed | CT/laparotomy/clinical follow-up | Any free fluid | 0.74 (0.65-0.81); children 0.63 (0.46-0.77) | 0.96 (0.94-0.98) | N/A | 34 studies | Reported in source | Cochrane methodology | At 28% prevalence, 73 injured adults and 118 injured children missed per 1000 scanned |
| Appendicitis: POCUS meta-analysis (Matthew Fields et al[35], 2017) | ED adults and children | Non-radiologist physicians; EP subgroup | Pathology/final diagnosis | Non-compressible, dilated appendix | 91% (83%-96%); EP subgroup 80% | 97% (91%-99%); EP subgroup 92% | N/A | 21/NR | 99% (99%-100%) | Not reported in retrievable text | Extreme heterogeneity; EP-only performance lower than the headline figure |
| Appendicitis: Paediatric meta-analysis (Miller et al[36], 2026) | Children | Mixed | Pathology/final diagnosis | Non-compressible, dilated appendix | 85.6% (68.9%-94.1%) | 90.2% | N/A | 8/993 | Sensitivity range 53%-100% across studies | Recent; see source | Between-study range wider than the pooled CI implies |
| Hydronephrosis/renal colic (Wong et al[37], 2018) | ED adults, suspected renal colic | EP | CT | Any hydronephrosis | 70.2% (67.1%-73.2%) | N/A | N/A | NR in retrievable text | NR in retrievable text | Not reported in retrievable text | Risk stratification only; cannot exclude |
| AAA (Shaban et al[34], 2025) | ED adults, symptomatic | EP | CT/operative/final diagnosis | Aortic diameter ≥ 3 cm (aneurysm definition) | 98.33% | 99.84% | N/A | 9/NR | NR in retrievable text | Not reported in retrievable text | Identifies an aneurysmal aorta; does NOT identify rupture, for which CT angiography is the reference standard |
Table 2 Tokyo Guidelines 2018 diagnostic and severity criteria relevant to bedside sonography
| Item | Acute cholecystitis | Acute cholangitis |
| Diagnostic criteria | One local sign of inflammation + one systemic sign = suspected; + characteristic imaging = definite[21] | One item of systemic inflammation + one item of cholestasis or imaging = suspected; all three = definite[88] |
| Systemic inflammation | N/A | Fever > 38 °C, or laboratory evidence of an inflammatory response[88] |
| Cholestasis | N/A | Jaundice with total bilirubin ≥ 2 mg/dL, or liver function tests > 1.5 × upper limit of normal[88] |
| Imaging item | Characteristic imaging findings (wall thickening ≥ 4 mm among them)[21] | Biliary dilatation, or evidence of aetiology (stricture, stone, stent)[88] |
| Grade I (mild) | No organ dysfunction; mild local inflammatory change[21] | Neither grade II nor grade III criteria met[88] |
| Grade II (moderate) | Any one of: WBC > 18000/mm³; palpable tender RUQ mass; complaints > 72 hours; marked local inflammation (gangrenous or emphysematous cholecystitis, pericholecystic or hepatic abscess, biliary peritonitis)[21] | Any two of five criteria, one of which is age ≥ 75 years[88] |
| Grade III (severe) | Dysfunction of any one organ system: Cardiovascular (hypotension requiring dopamine ≥ 5 μg/kg per minute, or any dose of noradrenaline); neurological (decreased consciousness); respiratory (PaO2/FiO2 < 300); renal (oliguria or creatinine > 2.0 mg/dL); hepatic (PT-INR > 1.5); haematological (platelets < 100000/mm³)[21] | Organ dysfunction as for cholecystitis[88] |
| Management by grade | Grade I and grade II (experienced surgeons): Early laparoscopic cholecystectomy where CCI ≤ 5 and ASA-PS ≤ 2; otherwise, medical treatment and/or gallbladder drainage with interval cholecystectomy. Grade III: Early or urgent biliary drainage with delayed cholecystectomy; upfront surgery only with favourable organ-system failure, no negative predictive factors, CCI ≤ 3, ASA-PS ≤ 2, in an advanced centre[81] | Biliary drainage, urgently in severe disease[88] |
| Sonographic component of grading | None: Grading uses vital signs, organ-failure laboratory values, WBC, symptom duration and comorbidity indices[21] | None[88] |
Table 3 The authors’ proposed specification: What a consensus process would need to fix before these applications can be standardised
| Consensus item | SBO | Gastric assessment | Free fluid beyond trauma | Biliary tract |
| Minimum image set | Number of quadrants required for a complete study is undefined; segmental obstruction means an incomplete survey can be falsely negative. Fix: Mandated quadrants and documented images per quadrant | Supine and RLD antral views are used inconsistently; some thresholds are supine-derived and others RLD-derived. Fix: Both positions mandatory, each documented | Number and identity of dependent recesses varies outside the FAST protocol; pelvic views may be omitted in non-trauma scanning. Fix: Defined recess set for the non-traumatic indication | Long-axis and short-axis gallbladder views, wall measurement site and duct view are not standardised. Fix: Mandated views including the point of wall measurement |
| Measurement convention | No published convention specifies outer-to-outer vs inner-to-inner, plane, or whether maximal or averaged loop diameter is used, a difference capable of exceeding the 2.5 mm separating the 2.5 cm and 2.75 cm thresholds. Fix: Single defined convention | Antral CSA is derived by different formulae and at different antral levels. Fix: One formula, one anatomical level, one patient position per stated threshold | Volume estimation and the distinction between trace, small, moderate and large collections are undefined; agreement falls to kappa 0.48-0.65 for this distinction. Fix: Defined volume categories with anchoring images | Wall thickness is measured at unspecified sites and on discordant scales, > 3 mm in the emergency literature against ≥ 4 mm in TG18. Fix: One threshold, one measurement site, one wall (anterior) |
| Definition of a positive study | Whether dilatation alone suffices, or dilatation plus abnormal peristalsis, or plus interloop fluid, varies between studies. Fix: Explicit rule for the composite | A positive study means different target volumes in different sources (empty stomach, > 1.25 mL/kg, aspiration-relevant content). Fix: State the target volume with the threshold | Any anechoic fluid vs a clinically significant volume is not distinguished. Fix: Population-specific definition, since physiological pelvic fluid differs by sex and pregnancy status | Number and combination of signs required is unstated; agreement is kappa 0.85 for gallstones but 0.37 for the composite diagnosis. Fix: Defined minimum criteria set, aligned to TG18 |
| Reporting lexicon | Terms for peristaltic patterns and the valvulae sign are used inconsistently across the literature. Fix: Controlled vocabulary with defined terms | Perlas grades 0-2 are well defined but quantitative and qualitative results are reported interchangeably. Fix: Report grade and CSA separately, never as equivalents | Descriptors of volume and location vary. Fix: Standardised recess names and volume categories | Sonographic Murphy sign has no standardised elicitation, defined transducer pressure or accounting for prior analgesia. Fix: Defined elicitation protocol, or removal of the sign from criteria |
| Reference standard | CT, surgical findings and final clinical diagnosis are used interchangeably across pooled studies. Fix: Single specified standard, or pre-specified stratification by standard | Aspirated volume, endoscopic volume and model-predicted volume are used as equivalents. Fix: One standard; and outcome studies linking measurement to aspiration rather than to volume | Trauma-derived standards (CT, laparotomy) are applied to non-traumatic populations. Fix: Indication-specific reference standard | Final diagnosis, pathology and TG18 give materially different specificity (17.1% vs 85%-94%). Fix: TG18 as the uniform standard, with the index test measured on the same scale |
| Training volume for credentialing | No application-specific minimum; the attending-resident sensitivity gap is 14.7 percentage points. Fix: Application-specific case minimum with competency assessment | No emergency-setting training standard exists; the available reliability study used three raters and healthy volunteers. Fix: Defined supervised case volume | FAST credentialing exists but is trauma-specific and does not cover non-traumatic indications. Fix: Extension of credentialing to the non-traumatic indication | Credentialing exists in most curricula but is not tied to demonstrated agreement on wall thickness or the Murphy sign. Fix: Competency demonstrated per sign, not per application |
| Quality assurance | No archived-image review requirement; loop measurement cannot be audited if images are not stored. Fix: Mandatory archiving of the measured loop | No QA mechanism described in any cited source. Fix: Archived antral images with periodic measurement audit | Where archiving exists it is trauma-oriented. Fix: QA review of non-traumatic studies, with attention to small collections | QA review is described in stewardship literature but is not sign-specific. Fix: Periodic audit of wall measurement and of Murphy-sign documentation |
| Priority reliability studies required | Inter-observer agreement for loop-diameter measurement: No published kappa or ICC was identified for this measurement, on which the entire branch turns | Inter-observer agreement for antral CSA in an emergency population; and any study linking measurement to aspiration rather than to volume | Inter-observer agreement for detecting a small collection in a non-traumatic emergency population, none identified | Inter-observer agreement for millimetre wall-thickness measurement in an emergency setting (none identified) and a second, multicentre study of the sonographic Murphy sign |
Table 4 Evidence-versus-proposal matrix for each action node of the integrated algorithm (Figure 1): What the node rests on, and whether it is derived from evidence or proposed by the authors
| Algorithm action node | Evidence type | Evidence supporting the node | Status | Ref. |
| Step 1: Instability/red-flag check precedes any scan | Expert recommendation | Consensus statements on emergency POCUS scope; no comparative trial of scan-first vs resuscitate-first | Authors’ proposal | Kameda and Taniguchi[7], Oto et al[8] |
| Step 2: Operator competency precondition | Evidence-informed | Operator-level subgroup estimates differ by application and do not all run the same way: For appendicitis the EP subgroup is lower than the pooled estimate on both axes (sensitivity 80% vs 91%, specificity 92% vs 97%), whereas for cholecystitis the EP subgroup matches the pooled sensitivity (71% vs 71%) and exceeds the pooled specificity (92% vs 85%). Competency is therefore required as a precondition because performance is operator-dependent in an application-specific direction, not because EP performance is uniformly lower | Evidence-based (subgroup estimates), authors’ proposal (credentialling requirement) | Huang et al[25], Matthew Fields et al[35] |
| Step 3: Symptom cluster sets pretest probability and orders the scans | Authors’ construction | No study compares symptom-ordered POCUS sequencing against a fixed protocol | Authors’ proposal | N/A |
| Biliary branch: Gallstones + sonographic Murphy sign + wall > 3 mm as the rule-in trigger | Evidence-based | Pooled specificity 94.4% (88.2%-97.5%) for EP-performed POCUS; TG18 uses wall ≥ 4 mm | Evidence-based | Yokoe et al[21], Wilson et al[32] |
| Biliary branch: Negative scan does not exclude cholecystitis | Evidence-based | Pooled EP sensitivity 70.9% (62.3%-78.2%); LR- accordingly poor | Evidence-based | Wilson et al[32] |
| Biliary branch; fever + jaundice + dilated duct triggers the cholangitis pathway | Guideline-based | TG18 diagnostic criteria (systemic inflammation + cholestasis + imaging) and severity grading | Evidence-based (guideline) | Okamoto et al[81], Kiriyama et al[88] |
| SBO branch: Dilated loops > 2.5 cm as the rule-in trigger | Evidence-based | Pooled sensitivity 92.4% (89.0%-94.7%), specificity 96.6% (88.4%-99.1%), LR+ 27.5 | Evidence-based | Gottlieb et al[9] |
| SBO branch: 2.75 cm as a candidate refined threshold | Authors’ construction | Proposed in a bedside-threshold analysis; no reliability data exist for bowel-loop diameter at this precision | Authors’ proposal: Explicitly unvalidated | Shokoohi et al[11] |
| SBO branch, CT still required for transition point, aetiology, ischaemia, perforation | Evidence-based | Consistent statement across the SBO syntheses; POCUS not evaluated for these endpoints | Evidence-based | Gottlieb et al[9], Shokoohi et al[10], Motavaselian et al[30] |
| Free-fluid branch, free fluid in Morison’s pouch or pelvis as the rule-in trigger | Evidence-based | Ectopic pregnancy cohort; prehospital FAST pooled specificity 0.970 (0.953-0.983) | Evidence-based | Lin et al[19], Moore et al[31] |
| Free-fluid branch: Ectopic pregnancy excluded only by seeing an intrauterine pregnancy | Evidence-based | Pooled FAST sensitivity 0.74 (0.65-0.81) in blunt trauma; absent free fluid carries no exclusionary value for ectopic pregnancy | Evidence-based | Stengel et al[18], Moore et al[31] |
| Aorta/renal branch, aortic diameter ≥ 3 cm; POCUS does not identify rupture | Evidence-based | Aneurysm detection sensitivity 98.3%, specificity 99.8%; no pooled estimate for rupture detection | Evidence-based | Shaban et al[34] |
| Gastric parallel branch: Perlas grade and antral CSA stratify aspiration risk | Evidence-based | IPD meta-analysis: Grade 0/1 gives 98% probability of being below the risk threshold; ED intubation cohort sensitivity 100%, specificity 87% | Evidence-based (against a surrogate endpoint) | Perlas et al[26], Asokan et al[27] |
| Gastric parallel branch; thresholds are position- and population-specific, not interchangeable | Evidence-based | Distinct CSA thresholds by position and population across the source studies | Evidence-based | Perlas et al[26] |
| Third exit; non-diagnostic study treated separately from a negative study | Authors’ construction | No source study reports a distinct action pathway for non-diagnostic examinations | Authors’ proposal, a principal original contribution | N/A |
| Serial scanning after an interval where the picture is evolving | Expert recommendation | No comparative evidence for serial abdominal POCUS in this setting | Authors’ proposal | N/A |
| Secondary redirect applications when the entry scan is negative or non-diagnostic | Evidence-based (component estimates), authors’ construction (the redirect rule) | Appendicitis EP sensitivity 80%, specificity 92%; hydronephrosis sensitivity 70.2%; AAA detection 98.3% | Mixed, estimates evidence-based, sequencing proposed | Shaban et al[34], Matthew Fields et al[35], Miller et al[36], Wong et al[37] |
| Governing principle, every application rules in better than it rules out | Evidence-based | Direct consequence of the sensitivity/specificity asymmetry documented in Table 1 | Evidence-based | Gottlieb et al[9], Shokoohi et al[10], Stengel et al[18], Lin et al[19], Huang et al[25], Wilson et al[32] |
- Citation: Danış F, Kudu E. Point-of-care ultrasound in the acute abdomen and gastrointestinal emergencies: An evidence-based guide and the case for standardisation. World J Gastrointest Surg 2026; 18(11): 125637
- URL: https://www.wjgnet.com/1948-9366/full/v18/i11/125637.htm
- DOI: https://dx.doi.org/10.4240/wjgs.125637